毕赤酵母
黄曲霉毒素
酶
聚丙烯酰胺凝胶电泳
生物化学
戒毒(替代医学)
十二烷基硫酸钠
化学
凝胶电泳
毕赤酵母
基因
色谱法
食品科学
生物
重组DNA
医学
病理
替代医学
作者
Li Li,Manxue Mei,Wang Jun,Jiang Huang,Xuyan Zong,Xiangyu Wang
标识
DOI:10.1002/biot.202300167
摘要
Abstract In this study, three aflatoxin degrading enzyme genes, tv‐adtz , arm‐adtz and cu‐adtz , were heterologously expressed in Pichia pastoris. The protein expression of the enzyme solution was detected by sodium dodecyl sulfate polyacrylamide gel electrophoresis, and the results showed that specific protein bands were detected and the target genes were successfully integrated into Pichia pastoris. The enzyme activities and detoxification efficiency of TV‐ADTZ, Arm‐ADTZ and Cu‐ADTZ crude enzyme solutions were detected, and the highest enzyme activities were up to 3.57, 4.30, and 2.41 U mL −1 , and the highest degradation rates were up to 45.58%, 60.0% and 34.21%, respectively. Arm‐ADTZ with the best degradation effect was selected and designed for detoxification application experiments to test its detoxification efficiency of AFB 1 in aqueous phase and in the process of moldy ground corn and preparation of DDGS, respectively, and the degradation rates reached 78.94%, 56.48%, and 24.31% after 24 h of reaction, respectively. Thus, it can be seen that the aflatoxin‐degrading enzyme gene was successfully integrated into Pichia pastoris and secreted for expression, and the expressed product could effectively degrade AFB 1 .
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